A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349117



Internal ID21006670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:184660001..184709500hg38UCSC Ensembl
chr2:185524728..185574227hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3849500
hg1949500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205345
Samples
Known GenesZNF804A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349117
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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